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一种黑色素瘤肿瘤抑制基因在11号染色体长臂23区的一个小(≤2兆碱基)区域的功能定位。

Functional localization of a melanoma tumor suppressor gene to a small (< or = 2 Mb) region on 11q23.

作者信息

Robertson G P, Goldberg E K, Lugo T G, Fountain J W

机构信息

Division of Biomedical Sciences, University of California, Riverside 92521, USA.

出版信息

Oncogene. 1999 May 20;18(20):3173-80. doi: 10.1038/sj.onc.1202664.

Abstract

We have previously demonstrated the existence of a melanoma tumor suppressor gene(s) on the long arm of chromosome 11 through suppression of tumorigenicity assays. Although loss of heterozygosity studies also support this finding, only a large critical region (44 cM) has been identified to date on 11q22-25. To further localize a tumor suppressor gene(s) within this region, we have now generated and characterized nine melanoma microcell hybrids, each retaining an introduced fragment of 11q. Of the nine hybrids, four were suppressed for tumor formation in nude mice, while five formed tumors at the same rate as the parental melanoma cell line (UACC 903). Molecular analysis of the hybrids with 118 microsatellite markers narrowed the location of a putative suppressor gene to a small (< or =2 Mb) candidate region on 11q23 between the markers D11S1786 and D11S2077 and within the larger region frequently deleted in melanoma tumors and cell lines. While multiple tumor suppressor genes are likely to reside on 11q22-25, the presence of this region in all four suppressed hybrids supports the simplest model that a single locus is responsible for the suppressed phenotype observed in UACC 903.

摘要

我们之前通过致瘤性抑制试验证明了11号染色体长臂上存在黑色素瘤肿瘤抑制基因。尽管杂合性缺失研究也支持这一发现,但迄今为止,仅在11q22 - 25上确定了一个大的关键区域(44厘摩)。为了进一步在该区域内定位肿瘤抑制基因,我们现已构建并鉴定了9个黑色素瘤微细胞杂种,每个杂种都保留了一条导入的11号染色体长臂片段。在这9个杂种中,有4个在裸鼠中形成肿瘤的能力受到抑制,而另外5个形成肿瘤的速度与亲代黑色素瘤细胞系(UACC 903)相同。利用118个微卫星标记对这些杂种进行分子分析,将一个假定的抑制基因的位置缩小到11q23上位于标记D11S1786和D11S2077之间且在黑色素瘤肿瘤和细胞系中经常缺失的较大区域内的一个小的(≤2兆碱基)候选区域。虽然多个肿瘤抑制基因可能位于11q22 - 25上,但在所有4个形成肿瘤能力受到抑制的杂种中都存在这个区域,这支持了最简单的模型,即单个基因座导致了在UACC 903中观察到的受抑制表型。

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